chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157613725157613726GA22GENIChomozygous112906742
4157613853157613854GT21GENIChomozygous112906744
4157614185157614186TG22GENIChomozygous112906746
4157614774157614775AT23GENIChomozygous112906748
4157616535157616536CA25GENIChomozygous112906752
4157619978157619979GT24GENIChomozygous112906754
4157620744157620745TC16GENIChomozygous112906756
4157621147157621148CT11GENIChomozygous112906758
4157623083157623084GA19GENIChomozygous112906760
4157625710157625711CT21GENIChomozygous112906762
4157626447157626448TC17GENIChomozygous112906764
4157627043157627044TC18GENIChomozygous112906766
4157629525157629526TC19GENIChomozygous112906768
4157631950157631951AG29GENIChomozygous112906772
4157633500157633501AG22GENIChomozygous112906776
4157634098157634099TC23GENIChomozygous112906778
4157635239157635240AC24GENIChomozygous112906780
4157637702157637703TA5GENIChomozygous126120548
4157639657157639658GC22GENIChomozygous112906786
4157644216157644217CG16GENIChomozygous112906788